Khaddour Karam, Haq Rizwan, Buchbinder Elizabeth I, Liu David, Manos Michael P, Ott Patrick A, Hodi F Stephen, Insco Megan L
Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, United States.
Melanoma Disease Center, Dana-Farber Cancer Institute, Boston, MA 02115, United States.
Oncologist. 2025 Mar 10;30(3). doi: 10.1093/oncolo/oyae297.
The biological and clinical relevance of gene fusions in melanoma is unknown. Reports and preclinical data have suggested that tumor cells with specific rearrangements such as RAF1 gene fusions could be therapeutically targeted. To investigate the relevance of targeted therapy in patients with melanoma harboring RAF1 gene fusions, we reviewed records of 1268 melanoma patients with targeted sequencing data at the Dana-Farber Cancer Institute. We identified 9 cases and report here on their clinicopathologic characteristics. We describe the favorable outcome of 2 patients who received MEK inhibitor therapy, including 1 patient with a durable response. We coalesced our data with published reports of patients with RAF1 gene fusions who were treated with targeted therapy. We find that single-agent MEK inhibition has anti-tumor activity in melanoma patients harboring an RAF1 gene fusion, and we propose that patients with RAF1 gene fusions should be considered for single-agent MEK inhibitor therapy.
基因融合在黑色素瘤中的生物学及临床相关性尚不清楚。报告及临床前数据表明,具有特定重排的肿瘤细胞,如RAF1基因融合细胞,可能是治疗的靶点。为了研究靶向治疗对携带RAF1基因融合的黑色素瘤患者的相关性,我们回顾了达纳-法伯癌症研究所1268例有靶向测序数据的黑色素瘤患者的记录。我们识别出9例患者,并在此报告他们的临床病理特征。我们描述了2例接受MEK抑制剂治疗患者的良好疗效,其中1例患者有持久反应。我们将我们的数据与已发表的接受靶向治疗的RAF1基因融合患者的报告进行了合并。我们发现单药MEK抑制对携带RAF1基因融合的黑色素瘤患者具有抗肿瘤活性,并且我们建议携带RAF1基因融合的患者应考虑接受单药MEK抑制剂治疗。